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WO2004048345A2 - Composes destines au traitement de l'obesite - Google Patents

Composes destines au traitement de l'obesite Download PDF

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Publication number
WO2004048345A2
WO2004048345A2 PCT/DK2003/000797 DK0300797W WO2004048345A2 WO 2004048345 A2 WO2004048345 A2 WO 2004048345A2 DK 0300797 W DK0300797 W DK 0300797W WO 2004048345 A2 WO2004048345 A2 WO 2004048345A2
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Prior art keywords
ylmethyl
compound according
amino
benzyl
alkyl
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PCT/DK2003/000797
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English (en)
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WO2004048345A3 (fr
Inventor
Kilian Waldemar Conde-Frieboes
Michael Ankersen
Ulrich Sensfuss
Birgitte Schjellerup Wulff
Henning THØGERSEN
Philipp Lustenberger
Klaus Rudolf
Bernd Krist
Stephan Müller
Dirk Stenkamp
Marcus Schindler
Heike Wieland
Kirsten Arndt
Original Assignee
Novo Nordisk A/S
Boehringer Ingelheim International Gmbh
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Application filed by Novo Nordisk A/S, Boehringer Ingelheim International Gmbh filed Critical Novo Nordisk A/S
Priority to CA002506843A priority Critical patent/CA2506843A1/fr
Priority to AU2003281978A priority patent/AU2003281978A1/en
Priority to JP2004554239A priority patent/JP2006515574A/ja
Priority to EP03773584A priority patent/EP1572669A2/fr
Publication of WO2004048345A2 publication Critical patent/WO2004048345A2/fr
Publication of WO2004048345A3 publication Critical patent/WO2004048345A3/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
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    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
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    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/26—Androgens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
    • A61P5/44—Glucocorticosteroids; Drugs increasing or potentiating the activity of glucocorticosteroids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/06—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members
    • C07D241/08—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Definitions

  • the present invention relates to novel compounds, pharmaceutical compositions containing them, use of the compounds for preparing medicaments for appetite regulation or for treating obesity and obesity related diseases as well as to a method for treatment of obesity and, consequently, for the treatment of obesity related diseases and conditions such as atherosclerosis, hypertension, diabetes, especially type 2 diabetes (NIDDM (non-insulin dependent diabetes mellitus)), impaired glucose tolerance (IGT), dyslipidaemia, coronary heart disease, gallbladder disease, osteoarthritis and various types of cancer such as endometrial, breast, prostate and colon cancers and the risk for premature death as well as other conditions, such as diseases and disorders, which conditions are improved by activation of the melanocortin receptors.
  • NIDDM non-insulin dependent diabetes mellitus
  • ITT impaired glucose tolerance
  • dyslipidaemia CAD
  • coronary heart disease gallbladder disease
  • osteoarthritis various types of cancer such as endometrial, breast, prostate and colon cancers and the risk for premature death as well as other conditions,
  • Obesity is a well known risk factor for the development of many very common diseases such as atherosclerosis, hypertension, type 2 diabetes (non-insulin dependent diabetes mellitus (NIDDM)), dyslipidaemia, coronary heart disease, and osteoarthritis and various malignancies. It also causes considerable problems through reduced motility and decreased quality of life. The incidence of obesity and thereby also these diseases is increasing throughout the entire industrialised world. Only a few pharmacological treatments are available to date, namely Sibutramine (acting via serotonergic and noradrenaline mechanisms, Abbott) and Orlistat (reducing fat uptake from the gut, Roche Pharm).
  • Sibutramine acting via serotonergic and noradrenaline mechanisms, Abbott
  • Orlistat reducing fat uptake from the gut, Roche Pharm.
  • obesity implies an excess of adipose tissue.
  • obesity is best viewed as any degree of excess adiposity that imparts a health risk.
  • BMI body mass index
  • Pro-opiomelanocortin is the precursor for ff-endorphin and melanocortin peptides, including melanocyte stimulating hormone ( ⁇ -MSH) and adrenocorticotropin (ACTH). POMC is expressed in several peripheral and central tissues including melanocytes, pituitary and neurones of the hypothalamus. The POMC precursor is processed differently in different tissues resulting in the expression of different melanocortin peptides depending on the site of expression.
  • ⁇ -MSH melanocyte stimulating hormone
  • ACTH adrenocorticotropin
  • MC1 , MC2, MC3, MC4 and MC5 A family of five melanocortin receptor subtypes has been identified (melanocortin receptor 1-5, also called MC1 , MC2, MC3, MC4 and MC5).
  • the MC1 , MC2 and MC5 are mainly expressed in peripheral tissues whereas MC3 and MC4 are mainly centrally expressed.
  • the MC4 receptor is shown to be involved in the regulation of body weight and feeding behaviour as MC4 knock out mice develop obesity (Huzar et al, Cell 88, 131-141 (1997)).
  • agouti MC1 , MC3 and MC4 antagonist
  • over-expression of an endogenously occurring MC3 and MC4 antagonist agouti gene related peptide, AGRP
  • a MC4 agonist could serve as an anorectic drug, and be useful in the treatment of obesity or obesity related diseases as well as in the treatment of other diseases, disorders or conditions, which are improved by activation of the MC4 receptor.
  • MC4 antagonists may be useful for treatment of cachaxia, anorexia, and for treatment of waisting in frail elderly patients.
  • MC4 antagonists may be used for treatment of chronic pain, neuropathy and neurogenic inflammation.
  • the present invention relates to novel compounds of the general formula (1),
  • A is -NR 2 R 3 or guanidinyl, the last optionally substituted with d-e-alkyl, wherein R 2 and R 3 independently of each other are hydrogen, d-e-alkyl,
  • R 11 and R 12 independently of each other are hydrogen or d- ⁇ -alkyl;
  • Z 1 is d- ⁇ -alkylene;
  • e is an integer selected from 0 or 1 ;
  • R 13 is cycloalkyl, heterocyclyl, aryl, or heteroaryl; each of which may be optionally substituted with a substitutent selected from the group consisting of d- 6 -alkyl, amino, and -CO-O-Z 4 -R 23 , wherein Z 4 is d- ⁇ -alkylene; and R 23 is aryl; and
  • R 14 is hydrogen, d- ⁇ -alkyl, -N(R 15 )(R 16 ), C 1 - 6 -alkylene-N(R 15 )(R 16 ), C(R 17 )(R 18 )-N(R 19 )(R 20 ), heterocyclyl, (Z 2 ) r R 21 , heteroaryl, or d- ⁇ -alkoxy, wherein
  • R 15 and R 16 independently of each other are hydrogen, or d- ⁇ -alkyl
  • R 17 and R 8 independently of each other are hydrogen, d-6-alkylene-NH 2 or (Z 3 ) g -R 22 ), wherein Z 3 is d- ⁇ -alkylene; g is an integer selected from 0 or 1 ; and R 22 is cycloalkyl, heterocyclyl, aryl or heteroaryl; R 19 and R 20 independently of each other are hydrogen, C 2 -6-alkylene-NH 2> C ⁇ - 6 -alkylene-CF 3 or cycloalkyl; and Z 2 is d- 6 -alkylene; f is an integer selected from 0 or 1 ; and R 2 is cycloalkyl, heterocyclyl, aryl or heteroaryl; a is an integer selected from 1 , 2, 3, 4, or 5;
  • E is cycloalkyl, heterocyclyl, aryl or heteroaryl; each of which may be optionally substituted with one or more substituents selected from the group consisting of halogen, hydroxy, cyano, nitro, -NR 4 R 5 , -CO-R 6 , d- ⁇ -alkyl, C ⁇ - 6 -alkoxy, trifluoromethyl, trifluoromethoxy, and wherein
  • R 4 and R 5 independently of each other are hydrogen, d- ⁇ -alkyl, -CO-R 24 , or aryl, wherein R 24 is hydrogen, d- 6 -alkyl or d. 6 -alkoxy;
  • R 6 is d-e-alkyl or d- 6 -alkoxy;
  • L 1 is a direct bond, -CH 2 -, -O-, -CO-, -CH 2 -O-, -O-CH 2 - or -NR 25 -, wherein
  • R 25 is hydrogen or d-e-alkyl
  • Q 1 is cycloalkyl, heterocyclyl, aryl or heteroaryl; each of which may be optionally substituted with one or more substituents selected from the group consisting of halogen, hydroxy, cyano, nitro, trifluoromethyl, trifluoromethoxy, -NR 26 R 27 , -CO-R 28 , -S(O) 2 -R 29 , d- 6 -alkyl, d- 6 -alkoxy, C 3 .
  • R 26 and R 27 independently of each other are hydrogen, d- ⁇ -alkyl, or -CO-R 30 , wherein R 30 is hydrogen, d- 6 -alkyl or d- ⁇ -alkoxy;
  • R 28 is d.6-alkyl or C ⁇ -alkoxy; and R 29 is d- 6 -alkyl, -NH-d- ⁇ -alkyl, or -N(C 1 - 6 -alky 2 ; or
  • Q 1 is L 3 -R 31 , wherein L 3 is -CH 2 -, -O-, -CO-, -CH 2 -O-, -O-CH 2 -, -CH 2 -O-C(O)-, or -C(O)-O-CH 2 -; and
  • R 31 is aryl or heteroaryl; b is an integer selected from 0, , or 2;
  • G 1 is d- ⁇ -alkyl, Ci- ⁇ -alkoxy, cycloalkyl, C 3 . 7 -cycloalkoxy, aryl or heteroaryl; each of which may be optionally substituted with halogen, hydroxy, cyano, nitro, trifluoromethyl, trifluoromethoxy, -NR 7 R 8 , d-e-alkyl, d- 6 -alkoxy, C 3 - 7 -cycloalkyl, C 3 . 7 -cycloalkoxy, wherein R 7 and R 8 independently of each other are hydrogen, d-e-alkyl, aryl, heteroaryl, -CO-R 32 or -SO 2 -R 33 , wherein
  • R 32 is hydrogen, d-e-alkyl or d- ⁇ -alkoxy; and R 33 is d- ⁇ -alkyl, -NH-d- ⁇ -alkyl. -N(d- 6 -alkyl) 2 ; G 2 is cycloalkyl, heterocyclyl, aryl, or heteroaryl; each of which may be optionally substituted with one or more substituents selected from the group consisting of halogen, hydroxy, cyano, nitro, difluoromethyl, trifluoromethyl, difluoromethoxy, trifluoromethoxy, -NR 9 R 10 , d- ⁇ -alkyl, d-e-alkoxy, C 3 . 7 -cycloalkyl, C 3 . 7 -cycloalkoxy or -L 2 -Q 2 , wherein
  • R 9 and R 1Q are independently hydrogen, d- ⁇ -alkyl, aryl, heteroaryl, -CO-R 34 or -S0 2 -R 35 , wherein
  • R 34 is hydrogen, d-e-alkyl or d-e-alkoxy; and R 35 is d- ⁇ -alkyl, -NH-d- ⁇ -alkyl. or -N(C 1 - 6 -alkyl) 2 ; L 2 is a direct bond, -CH 2 -, -O-, -CO-, -CH 2 -O-, -O-CH 2 - or -NR 36 -, wherein R 36 is hydrogen or d-e-alkyl; and Q 2 is cycloalkyl, heterocyclyl, aryl or heteroaryl; each of which may be optionally substituted with halogen, hydroxy, cyano, nitro, trifluoromethyl, -NR 37 R 38 , -CO-R 39 , -O-R 40 , Ci-e-alkyl, d-e-hydroxyalkyl, C 3 .
  • R 37 and R 38 independently of each other are hydrogen, Ci-e-alkyl or -CO-R 41 , wherein R 41 is hydrogen, d- 6 -alkyl or d-e-alkoxy;
  • R 39 is hydrogen, Ci-e-alkyl or d. 6 -alkoxy; and R 40 is Ci-e-alkyl or trifluoromethyl; c is an integer selected from 0, 1 , or 2; d is an integer selected from 0, or 1 ;and R 1 is hydrogen, alkyl, alkenyl, or alkynyl; well as any optical or geometric isomer or tautomer form thereof, or a pharmaeutically acceptable salt thereof.
  • the present invention also relates to pharmaceutical compositions containing compounds according to the present invention, use of compounds according to the present invention for preparing medicaments for appetite regulation or for treating obesity and obesity related diseases and to a method for treatment of obesity and, consequently, for the treatment of obesity related diseases and conditions such as atherosclerosis, hypertension, diabetes, especially type 2 diabetes (NIDDM (non-insulin dependent diabetes mellitus)), impaired glucose tolerance, dyslipidaemia, coronary heart disease, gallbladder disease, osteoarthritis and various types of cancer such as endometrial, breast, prostate and colon cancers and the risk for premature death as well as other conditions, such as diseases and disorders, which conditions are improved by activation of the MC4 receptor.
  • NIDDM non-insulin dependent diabetes mellitus
  • the present invention also relates to use of compounds according to the present invention for preparing medicaments for increasing skin pigmentation, for protecting the skin against ultraviolet radiation (UVR) and for inhibiting the effects of UVR, for protecting the skin against local skin irritants (e.g. bacterial lipopolysaccharide), for modulating the inflammatory responses in the skin, for functionally antagonising the actions of proinflammatory cytokines produced in the skin after a local irritation, for regulating the immune response, for preventing contact dermatitis, and for inhibiting chronic inflammatory responses.
  • the present invention also relates to use of compounds according to the present invention for regulating glucocorticoid production.
  • the present invention also relates to use of compounds according to the present invention for reducing blood pressure and heart rate and for inducing natriuresis.
  • the present invention also relates to use of compounds according to the present invention for regulating exocrine gland secretion, for regulating aldosterone secretion and thereby regulating blood pressure and natriuresis, for suppressing stress-induced alarm substances, and for stimulating exocrine glands, cardiac and testicular functions.
  • the present invention also relates to use of compounds according to the present invention for treating sexual dysfunction.
  • the present invention also relates to use of compounds according to the present invention for increasing antipyretic activity.
  • the present invention also relates to use of compounds according to the present invention for inducing lipolysis.
  • the present invention also relates to use of compounds according to the present invention for treating chronic pain.
  • Halogen designates an atom selected from the group consisting of F, Cl, Br or I.
  • C x - y -alkyl, C x - y -alkenyl, C x - y -alkynyl, C x . y - cycloalyl or C x . y -cycloalkyl-C x . y -alkenyl- designates radical of the designated type having from x to y carbon atoms.
  • alkyl refers to a straight or branched chain saturated monovalent hydrocarbon radical having from one to ten carbon atoms, for example Ci-e-alkyl.
  • Typical Ci-e-alkyl groups include, but are not limited to e.g.
  • Ci-a-alkyl as used herein also includes secondary C 3 . 8 -alkyl and tertiary d- ⁇ -alkyl.
  • C ⁇ - 6 -alkyl represents a straight or branched chain saturated monovalent hydrocarbon radical containing from 1 to 6 carbons atoms.
  • Representative examples for “d-e-alkyl” include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert- pentyl, n-hexyl, isohexyl and the like.
  • C ⁇ - ⁇ 8 -alkyl represent a straight or branched carbon chain containing from 1 to 18 carbons atoms.
  • alkylene refers to a straight or branched chain saturated divalent hydrocarbon radical having from one to ten carbon atoms, for example d-s-alkylene.
  • alkylene as used herein include, but are not limited to, methylene, ethylene, and the like.
  • alkoxy refers to the monovalent radical R a O-, where R a is alkyl as defined above, for example Ci-e-alkyl giving Ci-a-alkoxy.
  • Typical Ci-a-alkoxy groups include, but are not limited to, methoxy, ethoxy, n-propoxy, isopropoxy, butoxy, sec-butoxy, tert-butoxy, pentoxy, isopentoxy, hexoxy, isohexoxy and the like.
  • C ⁇ - 6 -alkoxy refers to the monovalent radical d-e-alkyl-O-, where Ci-e-alkyl is as defined above.
  • Representative examples are methoxy, ethoxy, n-propoxy, isopropoxy, butoxy, sec-butoxy, terf-butoxy, pentoxy, isopentoxy, hexoxy, isohexoxy and the like.
  • cycloalkyl refers to a non- aromatic monovalent hydrocarbon radical having from three to twelve carbon atoms, and optionally with one or more degrees of unsaturation, for example C 3 -s-cycloalkyl. Such a ring may be optionally fused to one or more benzene rings or to one or more of other cycloalkyl ring(s).
  • Typical C 3 -e-cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexenyl, cycloheptyl, cycloheptenyl, cyclooctyl and the like.
  • C 3 -e-cycloalkyl refers to a non- aromatic monovalent hydrocarbon radical having from 3 to 6 carbon atoms. Representative examples are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like.
  • heterocyclic or the term “heterocyclyl” as used herein, alone or in combination, refers to a heterocyclic ring with for instance three to thirteen member atoms, for example C 3 . ⁇ 0 -heterocyclyl, such as C 3 -e-heterocyclyl, having one or more degrees of unsaturation containing one or more heteroatomic substitutions selected from S, SO, SO 2 , O, or N, for example selected from N, O, or S.
  • Such a ring may be optionally fused to one or more of another "heterocyclic" ring(s) or cycloalkyl ring(s).
  • C 3 - ⁇ 0 - heterocyclyl or C 3 - 8 -heterocyclyl groups include, but are not limited to, pyrrolidinyl, piperidyl, piperazinyl, morpholinyl, thiomorpholinyl, aziridinyl, tetrahydrofuranyl and the like.
  • aryl refers to a carbocyclic aromatic ring radical or to a aromatic ring system radical with for instance six to thirteen member atoms, such as phenyl, biphenyl, naphthyl, anthracenyl, phenanthrenyl, fluorenyl, indenyl, pentalenyl, azulenyl, biphenylenyl, 5H-dibenzo[a,d]cyclohepten-5-yl, 10,11-dihydro- 5H-dibenzo[a,d]cyclohepten-5-yl and the like.
  • Aryl is also intended to include the partially hydrogenated derivatives of the carbocyclic systems enumerated above.
  • Non-limiting examples of such partially hydrogenated derivatives are 1 ,2,3,4-tetrahydronaphthyl, 1,4- dihydronaphthyl and the like.
  • aryloxy denotes a group aryl-O-, wherein aryl is as defined above.
  • heteroaryl refers to an aromatic ring radical with for instance 5 to 7 member atoms, or to an aromatic ring system radical with for instance from 7 to 18 member atoms, containing one or more heteroatoms selected from nitrogen, oxygen, or sulfur heteroatoms, wherein N-oxides and sulfur monoxides and sulfur dioxides are permissible heteroaromatic substitutions; such as e.g.
  • Heteroaryl is also intended to include the partially hydrogenated derivatives of the heterocyclic systems enumerated above.
  • Non-limiting examples of such partially hydrogenated derivatives are 2,3-dihydrobenzofuranyl, pyrrolinyl, pyrazolinyl, indolinyl, oxazolidinyl, oxazolinyl, oxazepinyl and the like.
  • hydroxyalkyl as used herein, alone or in combination, represents an alkyl radical as described above, such as a Ci- 6 -alkyl, substituted with one or more hydroxy radicals. Examples of Ci-e-hydroxyalkyl radicals are 2-hydroxymethyl, 2-hydroxyethyl, 2- hydroxypropyl, 3-hydroxypropyl, 2,3-dihydroxypropyl and the like.
  • a compound being a selective agonist of the MC3 receptor means that the compound does not bind or activate the other MC receptors, that is MC1 , MC2, MC4 and MC5.
  • a compound being a selective agonist of the MC4 receptor means that the compound does not bind or activate the other MC receptors, that is MC1 , MC2, MC3 and MC5.
  • a compound being a selective agonist of the MC5 receptor means that the compound does not bind or activate the other MC receptors, that is MC1 , MC2, MC3 and MC4.
  • a compound according to the present invention may also be said to be selective for two receptors, such as for instance the MC3 and MC4 receptor, meaning that the compound does not bind or activate the other MC receptors, in this case MC1, MC2, and MC5.
  • a “therapeutically effective amount” of a compound according to the present invention as used herein means an amount sufficient to cure, alleviate or partially arrest the clinical manifestations of a given disease and its complications. An amount adequate to accomplish this is defined as “therapeutically effective amount”. Effective amounts for each purpose will depend on the severity of the disease or injury as well as the weight and general state of the subject. It will be understood that determining an appropriate dosage may be achieved using routine experimentation, by constructing a matrix of values and testing different points in the matrix.
  • treatment means the management and care of a patient for the purpose of combating a condition, such as a disease or a disorder.
  • the term is intended to include the full spectrum of treatments for a given condition from which the patient is suffering, such as administration of the active compound to alleviate the symptoms or complications, to delay the progression of the disease, disorder or condition, to alleviate or relief the symptoms and complications, and/or to cure or eliminate the disease, disorder or condition as well as to prevent the condition, wherein prevention is to be understood as the management and care of a patient for the purpose of combating the disease, condition, or disorder and includes the administration of the active compounds to prevent the onset of the symptoms or complications.
  • the patient to be treated is preferably a mammal, in particular a human being.
  • NIDDM non-insulin dependent diabetes mellitus
  • compositions comprising the novel compounds of the invention being effective against obesity or obesity related diseases as described above as well as other conditions, such as diseases and disorders, which conditions are improved by activation of the MC4 receptor. Further objects will become apparent from the following description.
  • the invention relates to compounds according to formula (I)
  • A is -NR 2 R 3 or guanidinyl, the last optionally substituted with Ci-e-alkyl, wherein R 2 and R 3 independently of each other are hydrogen, Ci-e-alkyl, Ci. 6 -alkylene-N(R 11 )(R 12 ), C ⁇ - 6 -alkylene-CN, Ci-e-alkylene-OH, d- 6 -alkylene-C(O)-N(R 11 )(R 12 ), (Z 1 ) e -R 13 , or -CO-R 14 , wherein R 11 and R 2 independently of each other are hydrogen or C ⁇ . 6 -alkyl;
  • Z 1 is C ⁇ _ 6 -alkylene; e is an integer selected from 0 or 1 ; R 13 is cycloalkyl, heterocyclyl, aryl, or heteroaryl; each of which may be optionally substituted with a substitutent selected from the group consisting of Ci-e-alkyl, amino, and -CO-O-Z 4 -R 23 , wherein Z 4 is C ⁇ -6-alkylene; and R 23 is aryl; and
  • R 14 is hydrogen, Ci-e-alkyl, -N(R 15 )(R 16 ), C ⁇ - 6 -alkylene-N(R 15 )(R 16 ), C(R 17 )(R 18 )-N(R 19 )(R 20 ), heterocyclyl, (Z 2 ) r R 21 , heteroaryl, or d- ⁇ -alkoxy, wherein
  • R 15 and R 16 independently of each other are hydrogen, or Ci-e-alkyl
  • R 17 and R 18 independently of each other are hydrogen, C ⁇ -e-alkylene-NH 2 or (Z R 22 ), wherein Z 3 is d-e-alkylene; g is an integer selected from 0 or 1 ; and R 22 is cycloalkyl, heterocyclyl, aryl or heteroaryl;
  • R 19 and R 20 independently of each other are hydrogen, C 2 -e-alkylene-NH 2 , d-6-alkylene-CF 3 or cycloalkyl; and Z 2 is Ci-e-alkylene; f is an integer selected from 0 or 1 ; and R 21 is cycloalkyl, heterocyclyl, aryl or heteroaryl; a is an integer selected from 1 , 2, 3, 4, or 5;
  • E is cycloalkyl, heterocyclyl, aryl or heteroaryl; each of which may be optionally substituted with one or more substituents selected from the group consisting of halogen, hydroxy, cyano, nitro, -NR R 5 , -CO-R 6 , Ci-e-alkyl, C ⁇ -6-alkoxy, trifluoromethyl, trifluoromethoxy, and wherein
  • R 4 and R 5 independently of each other are hydrogen, Ci-e-alkyl, -CO-R 24 , or aryl, wherein
  • R 24 is hydrogen, d- 6 -alkyi or Ci-e-alkoxy; R 6 is Ci-e-alkyl or Ci-e-alkoxy; L 1 is a direct bond, -CH 2 -, -O-, -CO-, -CH 2 -O-, -O-CH 2 - or -NR 25 -, wherein
  • R 25 is hydrogen or Ci-e-alkyl; and Q 1 is cycloalkyl, heterocyclyl, aryl or heteroaryl; each of which may be optionally substituted with one or more substituents selected from the group consisting of halogen, hydroxy, cyano, nitro, trifluoromethyl, trifluoromethoxy, -NR 26 R 27 , -CO-R 28 , -S(O) 2 -R 29 , Ci-e-alkyl, Ci-e-alkoxy, C 3 . 7 -cycloalkyl and C 3 . 7 -cycloalkoxy, wherein R 26 and R 27 independently of each other are hydrogen, C ⁇ - 6 -alkyl, or -CO-R 30 , wherein
  • R 30 is hydrogen, C ⁇ - 6 -alkyl or C ⁇ - 6 -alkoxy;
  • R 28 is Ci-e-alkyl or Ci-e-alkoxy; and
  • R 29 is d- ⁇ -alkyl, -NH-d- 6 -alkyl, or -N(C ⁇ - 6 -alkyl) 2 ; or
  • Q 1 is L 3 -R 31 , wherein
  • L 3 is -CH 2 -, -O-, -CO-, -CH 2 -O-, -0-CH 2 -, -CH 2 -O-C(O)-, or -C(O)-O-CH r ; and R 31 is aryl or heteroaryl; b is an integer selected from 0, 1 , or 2;
  • G 1 is d-e-alkyl, Ci-e-alkoxy, cycloalkyl, d- cycloalkoxy, aryl or heteroaryl; each of which may be optionally substituted with halogen, hydroxy, cyano, nitro, trifluoromethyl, trifluoromethoxy, -NR 7 R 8 , Ci-e-alkyl, Ci-e-alkoxy, C3- 7 -cycloalkyl, C 3 . 7 -cycloalkoxy, wherein R 7 and R 8 independently of each other are hydrogen, Ci-e-alkyl, aryl, heteroaryl,
  • R 32 is hydrogen, Ci-e-alkyl or Ci-e-alkoxy; and R 33 is Ci-e-alkyl, -NH-d- ⁇ -alkyl, -N(C ⁇ -6-alkyl) 2 ;
  • G 2 is cycloalkyl, heterocyclyl, aryl, or heteroaryl; each of which may be optionally substituted with one or more substituents selected from the group consisting of halogen, hydroxy, cyano, nitro, difluoromethyl, trifluoromethyl, difluoromethoxy, trifluoromethoxy, -NR 9 R 10 , C ⁇ - 6 -alkyl, C ⁇ - 6 -alkoxy, C 3 . 7 -cycloalkyl, C 3 . -cycloalkoxy or -L 2 -Q 2 , wherein
  • R 9 and R 10 are independently hydrogen, Ci-e-alkyl, aryl, heteroaryl, -CO-R 34 or -SO 2 -R 35 , wherein R 34 is hydrogen, Ci-e-alkyl or C ⁇ . 6 -alkoxy;
  • R 35 is Cve-alkyl, -NH-d- ⁇ -alkyl, or -N(d- ⁇ -alkyl) 2 ;
  • L 2 is a direct bond, -CH 2 -, -O-, -CO-, -CH 2 -O-, -O-CH 2 - or -NR 36 -, wherein
  • R 36 is hydrogen or Ci-e-alkyl; and Q 2 is cycloalkyl, heterocyclyl, aryl or heteroaryl; each of which may be optionally substituted with halogen, hydroxy, cyano, nitro, trifluoromethyl, -NR 37 R 38 , -CO-R 39 ,
  • Ci-e-alkyl Ci-e-hydroxyalkyl, C 3 . 7 -cycloalkyl or C ⁇ -cycloalkoxy, wherein R 37 and R 38 independently of each other are hydrogen, Ci-e-alkyl or -CO-R 41 , wherein
  • R 41 is hydrogen, C ⁇ - 6 -alkyl or Ci-e-alkoxy
  • R 39 is hydrogen, Ci-e-alkyl or Ci-e-alkoxy
  • R 40 is Ci-e-alkyl or trifluoromethyl; c is an integer selected from 0, 1 , or 2; d is an integer selected from 0, or 1 ;and R is hydrogen, alkyl, alkenyl, or alkynyl; as well as any optical or geometric isomer or tautomer form thereof, or a pharmaeutically acceptable salt thereof.
  • the compounds of the present invention may have one or more asymmetric centres and it is intended that stereoisomers (optical isomers), as separated, pure or partially purified stereoisomers or racemic mixtures thereof are included in the scope of the invention.
  • the compound is an agonist of a melanocortin receptor, such as the MC4 receptor.
  • the compound is an intermediate in the synthesis of a agonist of a melanocortin receptor, such as the MC4 receptor.
  • the compound is selective for the MC4 receptor.
  • the present invention relates to a pharmaceutical composition comprising, as an active ingredient, at least one compound according to the present invention together with one or more pharmaceutically acceptable carriers or excipients.
  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising, as an active ingredient, at least one compound according to the present invention together with one or more pharmaceutically acceptable carriers or excipients in unit dosage form, comprising from about 0.05 mg to about 1000 mg, such as about 0.1 mg to about 500 mg, for example from about 0.5 mg to about 200 mg of a compound according to the present invention.
  • the present invention relates to the use of a compound according to the present invention for increasing the activity of the MC4 receptor. In one embodiment, the present invention relates to the use of a compound according to the present invention for the delaying or prevention of the progression from IGT to type 2 diabetes.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for the delaying or prevention of the progression from IGT to type 2 diabetes. In one embodiment, the present invention relates to the use of a compound according to the present invention for the delaying or prevention of the progression from non- insulin requiring type 2 diabetes to insulin requiring type 2 diabetes.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for the delaying or prevention of the progression from non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes.
  • the present invention relates to the use of a compound according to the present invention for treating a condition which is improved by the activation of the MC4 receptor.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treating a condition which is improved by the activation of the MC4 receptor.
  • the present invention relates to the use of a compound according to the present invention for appetite regulation.
  • the present invention relates to the use of a compound according to the present invention for treating a condition related to overweight or obesity.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for appetite regulation.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treating a condition related to overweight or obesity.
  • the present invention relates to the use of a compound according to the present invention for treating a disease or condition selected from overweight or obesity, atherosclerosis, hypertension, diabetes, type 2 diabetes, impaired glucose tolerance, dyslipidaemia, coronary heart disease, gallbladder disease, osteoarthritis, cancer, sexual dysfunction and the risk for premature death in a patient in need thereof.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treating a disease or condition selected from overweight or obesity, atherosclerosis, hypertension, diabetes, type 2 diabetes, impaired glucose tolerance, dyslipidaemia, coronary heart disease, gallbladder disease, osteoarthritis, cancer, sexual dysfunction and the risk for premature death in a patient in need thereof.
  • the present invention relates to the use of a compound according to the present invention for treating overweight or obesity.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treating overweight or obesity.
  • the present invention relates to the use of a compound according to the present invention for treating type 2 diabetes, for instance in obese patients.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treating type 2 diabetes, for instance in obese patients.
  • the present invention relates to the use of a compound according to the present invention for treating dyslipidemia, for instance in obese patients.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treating dyslipidemia, for instance in obese patients.
  • the present invention relates to the use of a compound according to the present invention for treating sexual dysfunction.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treating sexual dysfunction.
  • the present invention relates to the use of a compound according to the present invention for reducing the weight of a subject.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for reducing the weight of a subject.
  • the present invention relates to the use of a compound according to the present invention for the suppression of appetite or for satiety induction.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for the suppression of appetite or for satiety induction.
  • the present invention relates to the use of a compound according to the present invention for treatment of eating disorders such as bulimia and binge eating.
  • the present invention relates to the use of a compound according to the present invention for the preparation of a medicament for treatment of eating disorders such as bulimia and binge eating.
  • the invention relates to a method for the treatment of disorders related to melanocortin MC4 receptor, the method comprising administering to a subject in need thereof an effective amount of a compound according to formula (I)
  • the invention relates to a method for the treatment of obesity, the method comprising administering to a subject in need thereof an effective amount of a compound according to formula (I) or a pharmaceutically acceptable salt thereof, or of a composition according to any one of the preceding composition claims.
  • the invention relates to a method for the treatment of diabetes, preferably type 2 diabetes, the method comprising administering to a subject in need thereof an effective amount of a compound according to formula (I) or a pharmaceutically acceptable salt thereof, or of a composition according to any one of the preceding composition claims.
  • the invention relates to the use of a compound according to formula (I) or a pharmaceutically acceptable salt thereof for the preparation of a medicament. Furthermore the invention relates to the use of a compound according to formula (I) or a pharmaceutically acceptable salt thereof for the preparation of a medicament for the treatment of disorders related to melanocortin MC4 receptor.
  • the invention relates to the use of a compound according formula (I) or a pharmaceutically acceptable salt thereof for the preparation of a medicament having melanocortin MC4 agonist activity.
  • the invention relates furthermore to the use of a compound according to formula (I) or a pharmaceutically acceptable salt thereof for the preparation of a medicament for the treatment of obesity.
  • the invention relates furthermore to the use of a compound according to formula (I) or a pharmaceutically acceptable salt thereof for the preparation of a medicament for the treatment of diabetes preferably type 2 diabetes.
  • Such treatment includes inter alia treatment for the purpose of delaying or prevention of the progression from IGT to type 2 diabetes as well as delaying or prevention of the progression from non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes.
  • the invention relates furthermore to the use of a compound according to formula (I) or a pharmaceutically acceptable salt thereof for the preparation of a medicament for the treatment of obesity and complications related to obesity and excessive food consumption and other eating disorders and specific complications related to obesity, such as hypertension, dyslipidemia, diabetes mellitus, coronary heart disease, congestive heart failure, stroke, gallstones, osteoarthritis, sleep apnea, cancer, women's health/reproduction (within this area is noted psychopathology of obesity, such as body image and binge eating).
  • a compound according to formula (I) or a pharmaceutically acceptable salt thereof for the preparation of a medicament for the treatment of obesity and complications related to obesity and excessive food consumption and other eating disorders and specific complications related to obesity, such as hypertension, dyslipidemia, diabetes mellitus, coronary heart disease, congestive heart failure, stroke, gallstones, osteoarthritis, sleep apnea, cancer, women's health/reproduction (within this area is noted psychopathology of obesity, such
  • the compounds according to formula (I) may be useful for stimulation of melanin-production, skin darkening, inflammation, body temperature, pain perception, neuropathy, blood pressure, heart rate, vascular tone, natruresis, brain blood flow, nerve growth, placental development, aldosteron synthesis and release, thyroxin release, spermatogenesis, ovarian weight, prolactin, growth hormone and FSH secretion, uterine bleeding in women, sebum and pheromone secretion, blood glucose levels, intrauterine foetal growth, as well as other related to parturition, and to afford neuroprotective effects and for the treatment of eating disorders, improvement of libido activity in male and female and for stimulation of penile erection as well as psychiatric disorders, (such as depression, anxiety, motivational defects, cognitive disorders, memory loss and other psychiatric disorders as known by those skilled in the art), as well as addiction.
  • psychiatric disorders such as depression, anxiety, motivational defects, cognitive
  • the present invention also provides pharmaceutical compositions comprising as an active ingredient, at least one compound, preferably in a pharmacologically effective amount, more preferably in a therapeutically effective amount, suitable for any of the uses according to the present invention together with one or more pharmaceutically acceptable carriers or excipients.
  • a compound according to the present invention may also be administered in combination with one or more further active substances in any suitable ratios.
  • Such further active agents may be selected from antidiabetic agents, antihypieripidemic agents, antiobesity agents, antihypertensive agents and agents for the treatment of complications resulting from or associated with diabetes.
  • Suitable antidiabetic agents include insulin, GLP-1 (glucagon like peptide-1) derivatives such as those disclosed in WO 98/08871 (Novo Nordisk A/S), which is incorporated herein by reference, as well as orally active hypoglycemic agents.
  • Suitable orally active hypoglycemic agents include imidazolines, sulfonylureas, biguanides, meglitinides, oxadiazolidinediones, thiazolidinediones, insulin sensitizers, a- glucosidase inhibitors, agents acting on the ATP-dependent potassium channel of the pancreatic ⁇ -cells eg potassium channel openers such as those disclosed in WO 97/26265, WO 99/03861 and WO 00/37474 (Novo Nordisk A/S) which are incorporated herein by reference, potassium channel openers, such as ormitiglinide, potassium channel blockers such as nateglinide or BTS-67582, glucagon antagonists such as those disclosed in WO 99/01423 and WO 00/39088 (Novo Nordisk A/S and Agouron Pharmaceuticals, Inc.), all of which are incorporated herein by reference, GLP-1 agonists such as those disclosed in WO
  • the compound involved may be administered in combination with insulin or insulin analogues.
  • the compound involved may be administered in combination with a sulphonylurea eg tolbutamide, chlorpropamide, tolazamide, glibenclamide, glipizide, glimepiride, glicazide or glyburide.
  • a sulphonylurea eg tolbutamide, chlorpropamide, tolazamide, glibenclamide, glipizide, glimepiride, glicazide or glyburide.
  • the compound involved may be administered in combination with a biguanide eg metformin.
  • the compound involved may be administered in combination with a meglitinide eg repaglinide or senaglinide/nateglinide.
  • a meglitinide eg repaglinide or senaglinide/nateglinide.
  • the compound involved may be administered in combination with a thiazolidinedione insulin sensitizer eg troglitazone, ciglitazone, pioglitazone, rosiglitazone, isaglitazone, darglitazone, englitazone, CS-011/CI-1037 or T 174 or the compounds disclosed in WO 97/41097 (DRF-2344), WO 97/41119, WO 97/41120, WO 00/41121 and WO 98/45292 (Dr. Reddy's Research Foundation), which are incorporated herein by reference.
  • a thiazolidinedione insulin sensitizer eg troglitazone, ciglitazone, pioglitazone, rosiglitazone, isaglitazone, darglitazone, englitazone, CS-011/CI-1037 or T 174 or the compounds disclosed in WO 97/41097 (DRF-2344), WO
  • the compound involved may be administered in combination with an insulin sensitizer eg such as Gl 262570, YM-440, MCC-555, JTT-501 , AR-H039242, KRP-297, GW-409544, CRE-16336, AR-H049020, LY510929, MBX-102, CLX-0940, GW-501516 or the compounds disclosed in WO 99/19313 (NN622/DRF-2725), WO 00/50414, WO 00/63191 , WO 00/63192, WO 00/63193 (Dr.
  • an insulin sensitizer eg such as Gl 262570, YM-440, MCC-555, JTT-501 , AR-H039242, KRP-297, GW-409544, CRE-16336, AR-H049020, LY510929, MBX-102, CLX-0940, GW-501516 or the compounds disclosed in WO 99/19313 (NN622/
  • the compound involved may be administered in combination with an ⁇ -glucosidase inhibitor eg voglibose, emiglitate, miglitol or acarbose.
  • the compound involved may be administered in combination with a glycogen phosphorylase inhibitor eg the compounds described in WO 97/09040 (Novo Nordisk A/S).
  • the compound involved may be administered in combination with a glucokinase activator.
  • the compound involved may be administered in combination with an agent acting on the ATP-dependent potassium channel of the pancreatic ⁇ -cells eg tolbutamide, glibenclamide, glipizide, glicazide, BTS-67582 or repaglinide. In one embodiment of the uses and methods of the present invention, the compound involved may be administered in combination with nateglinide.
  • an agent acting on the ATP-dependent potassium channel of the pancreatic ⁇ -cells eg tolbutamide, glibenclamide, glipizide, glicazide, BTS-67582 or repaglinide.
  • the compound involved may be administered in combination with nateglinide.
  • the compound involved may be administered in combination with an antihyperiipidemic agent or a antilipidemic agent eg cholestyramine, colestipol, clofibrate, gemfibrozil, lovastatin, pravastatin, simvastatin, probucol or dextrothyroxine.
  • an antihypieripidemic agent eg cholestyramine, colestipol, clofibrate, gemfibrozil, lovastatin, pravastatin, simvastatin, probucol or dextrothyroxine.
  • the compound involved may be administered in combination with more than one of the above-mentioned compounds eg in combination with metformin and a sulphonylurea such as glyburide; a sulphonylurea and acarbose; nateglinide and metformin; acarbose and metformin; a sulfonylurea, metformin and troglitazone; insulin and a sulfonylurea; insulin and metformin; insulin, metformin and a sulfonylurea; insulin and troglitazone; insulin and lovastatin; etc.
  • a sulphonylurea such as glyburide
  • a sulphonylurea and acarbose such as glyburide
  • a sulphonylurea and acarbose such as glyburide
  • the compound involved may be administered in combination with one or more antiobesity agents or appetite regulating agents.
  • agents may be selected from the group consisting of CART (cocaine amphetamine regulated transcript) agonists, NPY (neuropeptide Y) antagonists, orexin antagonists, TNF (tumor necrosis factor) agonists, CRF (corticotropin releasing factor) agonists, CRF BP (corticotropin releasing factor binding protein) antagonists, urocortin agonists, /?3 adrenergic agonists such as CL-316243, AJ-9677, GW-0604, LY362884, LY377267 or AZ-40140, MSH (melanocyte-stimulating hormone) agonists, MCH
  • melanocyte-concentrating hormone antagonists CCK (cholecystokinin) agonists, serotonin reuptake inhibitors (fluoxetine, seroxat or citalopram), serotonin and norepinephrine reuptake inhibitors, 5HT (serotonin) agonists, bombesin agonists, galanin antagonists, growth hormone, growth factors such as prolactin or placental lactogen, growth hormone releasing compounds, TRH (thyreotropin releasing hormone) agonists, UCP 2 or 3 (uncoupling protein 2 or 3) modulators, leptin agonists, DA (dopamine) agonists (bromocriptin, doprexin), lipase/amylase inhibitors, PPAR modulators, RXR modulators, TR ⁇ agonists, adrenergic CNS stimulating agents, AGRP (agouti related protein) inhibitors, H3 histamine antagonists such as those disclosed in WO 00/
  • antiobesity agents are bupropion (antidepressant), topiramate (anticonvulsant), ecopipam (dopamine D1/D5 antagonist), naltrexone (opioid antagonist), and peptide YY 3 . 36 (Batterham et al, Nature 418, 650-654 (2002)).
  • the antiobesity agent is leptin.
  • the antiobesity agent is peptide YY 3 ⁇ 6 - In one embodiment, the antiobesity agent is a serotonin and norepinephrine reuptake inhibitor eg sibutramine.
  • the antiobesity agent is a lipase inhibitor eg orlistat.
  • the antiobesity agent is an adrenergic CNS stimulating agent eg dexamphetamine, amphetamine, phentermine, mazindol phendimetrazine, diethylpropion, fenfluramine or dexfenfluramine.
  • an adrenergic CNS stimulating agent eg dexamphetamine, amphetamine, phentermine, mazindol phendimetrazine, diethylpropion, fenfluramine or dexfenfluramine.
  • the compound involved may be administered in combination with one or more antihypertensive agents.
  • antihypertensive agents are ⁇ -blockers such as alprenolol, atenolol, timolol, pindolol, propranolol and metoprolol, ACE (angiotensin converting enzyme) inhibitors such as benazepril, captopril, enalapril, fosinopril, lisinopril, quinapril and ramipril, calcium channel blockers such as nifedipine, felodipine, nicardipine, isradipine, nimodipine, diltiazem and verapamil, and ⁇ -blockers such as doxazosin, urapidil, prazosin and terazosin.
  • ⁇ -blockers such as alprenolol, atenolol, timolol, pin
  • the present invention includes within its scope pharmaceutical compositions comprising, as an active ingredient, at least one of the compounds of the general formula (I) or a pharmaceutically acceptable salt thereof together with a pharmaceutically acceptable carrier or diluent.
  • the pharmaceutical composition of the invention may comprise a compound of formula (I) combined with one or more compounds.
  • compositions containing a compound of the present invention may be prepared by conventional techniques, e.g. as described in Remington: The Science and Practise of Pharmacy, 19 th Ed., 1995.
  • the compositions may appear in conventional forms, for example capsules, tablets, aerosols, solutions, suspensions or topical applications.
  • Typical compositions include a compound of formula (I) or a pharmaceutically acceptable acid addition salt thereof, associated with a pharmaceutically acceptable excipient which may be a carrier or a diluent or be diluted by a carrier, or enclosed within a carrier which can be in the form of a capsule, sachet, paper or other container.
  • conventional techniques for the preparation of pharmaceutical compositions may be used.
  • the active compound will usually be mixed with a carrier, or diluted by a carrier, or enclosed within a carrier which may be in the form of a ampoule, capsule, sachet, paper, or other container.
  • a carrier which may be in the form of a ampoule, capsule, sachet, paper, or other container.
  • the carrier serves as a diluent, it may be solid, semi-solid, or liquid material which acts as a vehicle, excipient, or medium for the active compound.
  • the active compound can be adsorbed on a granular solid container for example in a sachet.
  • suitable carriers are water, salt solutions, alcohols, polyethylene glycols, polyhydroxyethoxylated castor oil, peanut oil, olive oil, gelatine, lactose, terra alba, sucrose, cyclodextrin, amylose, magnesium stearate, talc, gelatin, agar, pectin, acacia, stearic acid or lower alkyl ethers of cellulose, silicic acid, fatty acids, fatty acid amines, fatty acid monoglycerides and diglycerides, pentaerythritol fatty acid esters, polyoxyethylene, hydroxymethylcellulose and polyvinylpyrrolidone.
  • the carrier or diluent may include any sustained release material known in the art, such as glyceryl monostearate or glyceryl distearate, alone or mixed with a wax.
  • the formulations may also include wetting agents, emulsifying and suspending agents, preserving agents, sweetening agents or flavouring agents.
  • the formulations of the invention may be formulated so as to provide quick, sustained, or delayed release of the active ingredient after administration to the patient by employing procedures well known in the art.
  • compositions can be sterilized and mixed, if desired, with auxiliary agents, emulsifiers, salt for influencing osmotic pressure, buffers and/or colouring substances and the like, which do not deleteriously react with the active compounds.
  • the route of administration may be any route, which effectively transports the active compound to the appropriate or desired site of action, such as oral, nasal, pulmonary, buccal, subdermal, intradermal, transdermal or parenteral e.g. rectal, depot, subcutaneous, intravenous, intraurethral, intramuscular, intranasal, ophthalmic solution or an ointment, the oral route being preferred.
  • a solid carrier is used for oral administration, the preparation may be tabletted, placed in a hard gelatin capsule in powder or pellet form or it can be in the form of a troche or lozenge.
  • a liquid carrier is used, the preparation may be in the form of a syrup, emulsion, soft gelatin capsule or sterile injectable liquid such as an aqueous or non-aqueous liquid suspension or solution.
  • the preparation may contain a compound of formula (I) dissolved or suspended in a liquid carrier, in particular an aqueous carrier, for aerosol application.
  • a liquid carrier in particular an aqueous carrier
  • the carrier may contain additives such as solubilizing agents, e.g. propylene glycol, surfactants, absorption enhancers such as lecithin (phosphatidylcholine) or cyclodextrin, or preservatives such as parabenes.
  • injectable solutions or suspensions preferably aqueous solutions with the active compound dissolved in polyhydroxylated castor oil.
  • Tablets, dragees, or capsules having talc and/or a carbohydrate carrier or binder or the like are particularly suitable for oral application.
  • Preferable carriers for tablets, dragees, or capsules include lactose, corn starch, and/or potato starch.
  • a syrup or elixir can be used in cases where a sweetened vehicle can be employed.
  • a typical tablet which may be prepared by conventional tabletting techniques may contain: Core:
  • Active compound 250 mg
  • the compounds of the invention may be administered to a mammal, especially a human in need of such treatment, such as prevention, elimination, alleviation or amelioration of obesity.
  • mammals include also animals, both domestic animals, e.g. household pets, and non-domestic animals such as wildlife.
  • the compounds of the invention may be effective over a wide dosage range. For example, in the treatment of adult humans, dosages from about 0.05 to about 1000 mg, for example from about 0.1 to about 500 mg, such as from about 0.5 mg to about 250 mg per day may be used. In choosing a regimen for patients it may frequently be necessary to begin with a higher dosage and when the condition is under control to reduce the dosage.
  • the exact dosage will depend upon the mode of administration, on the therapy desired, form in which administered, the subject to be treated and the body weight of the subject to be treated, and the preference and experience of the physician or veterinarian in charge.
  • a dosage of for instance from 1 to 100 mg/kg body weight, for example 10 mg/kg body weight pr day may be used.
  • the compounds of the present invention are dispensed in unit dosage form comprising from about 0.05 to about 1000 mg of active ingredient together with a pharmaceutically acceptable carrier per unit dosage.
  • dosage forms suitable for oral, nasal, pulmonal or transdermal administration comprise from about 0.05 mg to about 1000 mg, such as from about 0.5 mg to about 250 mg of the compounds of formula (I) admixed with a pharmaceutically acceptable carrier or diluent.
  • SciexAP1 100 Single quadropole mass spectrometer Perkin Elmer Series 200 Quard pump • Perkin Elmer Series 200 autosampler
  • the instrument control and data acquisition are done by the SciexSample control software running on a Macintosh PowerPC 7200 computer.
  • the HPLC pump is connected to four eluent reservoirs containing:
  • the requirements for samples are that they contain approximately 500 ⁇ g/ml of the compound to be analysed in an acceptable solvent such as methanol, ethanol, acetonitrile, THF, water and mixtures thereof. (High concentrations of strongly eluting solvents will interfere with the chromatography at low acetonitrile concentration.)
  • the analysis is performed at room temperature by injecting 20 ⁇ l of the sample solution on the column which is eluted with a gradient of acetonitrile in either 0.05% TFA or 0.002 M ammonium acetate. Depending on the analysis method varying elution conditions are used.
  • the eluate from the column is passed through a flow splitting T-connector which passed approximately 20 ⁇ l/min (1/50) through approx. 1 m. 75 ⁇ m fused silica capillary to the API interface of API 100 spectrometer.
  • the remaining 1.48 ml/min (49/50) is passed through the UV detector and to the ELS detector.
  • the detection data are acquired concurrently from mass spectrometer, UV detector and ELS detector.
  • HPLC-MS (Method B) This method is identical to HPLC-MS (Method A) but using the following conditions and settings:
  • the instrument is controlled by HP Chemstation software.
  • the HPLC pump is connected to two eluent reservoirs containing: A: 0.01% TFA in water
  • the analysis is performed at 40°C by injecting an appropriate volume af the sample (preferably 1 ⁇ l) onto the column which is eluted with a gradient of acetonitrile.
  • HPLC conditions, detector settings and mass spectrometer settings usded are giving in the following table.
  • the analysis is performed at room temperature by injecting an appropriate volume of the sample (preferably 10 ⁇ l) onto the column, which is eluted, with a gradient of acetonitrile.
  • the eluate from the column passed through the UV detector to meet a flow splitter, which passed approximately 30 ⁇ l/min (1/50) through to the API Turbo ion-spray interface of API 3000 spectrometer. The remaining 1.48 ml/min (49/50) is passed through to the ELS detector.
  • HPLC conditions, detector settings and mass spectrometer settings used are giving in the following table.
  • Step B Add 1500 ⁇ l of a 1:1 mixture of DMF and piperidine to the resin, shake for 30 min and wash 6 times with 1800 ⁇ l DMF.
  • Step A 10 mmol amino acid methyl ester hydrochloride, 1 equi. aldehyde and 1 equi. DIPEA are suspended in 100 ml THF and the resulting mixture is stirred overnight. Then 2.9 equi. NaCNBH 3 , 10 ml MeOH and 5 ml HOAc are added and stirred for 3 h. The solvent is removed in vacuo and the residual oil is taken up in 100 ml ethyl acetate. The org. phase is washed once with 100 ml 1M NaOH. The aq. phase is extracted once with 100 ml ethyl acetate and the combined org. phases are dried over sodium sulfate. The solvent is removed in vacuo and the crude product is used for the next step.
  • Step C 18.4 mmol Boc-protected amino acid is dissolved in 50 ml THF, 0.5 equi. DIC is added and the resulting mixture is stirred for 20 min. Then the crude product of step A is added in 50 ml THF and stirred for 2 h. Another 0.25 equi. DIC is added and after 20 min 2 ml of DIPEA. The solvent is removed after 3 h of stirring and the residue is taken up in 100 ml ethyl acetate. The org. phase is washed with 100 ml 1 M HCl and 100 ml sat. NaHCO 3 and dried over sodium sulfate. The solvent is removed in vacuo and the residual oil is purified on silica with ethyl acetate/heptane. Step C:
  • the purified product from step B is dissolved in 100 ml DCM and 100 ml TFA is added. The solvents are removed after 2 h. The residual oil is taken up in 100 ml toluene and the solvent is again removed in vacuo. The oil is taken up in 100 ml DCM and 1 ml DIPEA is added. The solvent is removed in vacuo and the product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1 % TFA in water and acetonitril.
  • a linker on polystyrene is prepared by stirring 20 g hydroxymethyl polystyrene (loading 0.87 mmol/g) with 11.3 g (4 equi.) carbonyldiimidazol (CDI) in 500 ml tetrahydrofuran (THF) for 17 h. Wash the resin then with dichloromethane and take it up in 500 ml N-methyl pyrrolidone (NMP). Add 5.3 ml (4 equi) amino propanol and stirr the mixture over night. Wash the resin once with methanol and once with dichloromethane. Repeat the two washing steps twice (3x(1xMeOH,1xCH 2 CI 2 )). Wash the resin once with diethylether and dry it in vacuo.
  • CDI carbonyldiimidazol
  • Step D Add 1000 ⁇ l NMP and 1000 ⁇ l piperidine and shake the mixture for 30 min. Wash the resin 5 times with 3000 ⁇ l NMP.
  • a intermediate product is synthesised according to general procedure B using Boc- Tyr(-'-bu)-OH for the acylation in step C.
  • Step B The product of step A (14 mmol) is dissolved in 100 ml DCM and 2 equi., 6.1 ml
  • step B The product of step B (1 mmol) is dissolved in 10 ml THF and 1 equi., 0.3 g triphenylphosphine and 1 equi. alcohol are added. Then 1 equi., 160 ⁇ l diethyl azadicarboxylate are added and the mixture is stirred over night. The solvent is removed in vacuo and the product is purified either on reverse phase or silica.
  • step C The product of step C (0.5 mmol) is dissolved in 25 ml DCM and 25 ml TFA. The solvent is removed after 30 min and the solvents are removed in vacuo. The product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • step B (10 mmol), amino acid methyl ester (10 mmol), TBTU (10.4 mmol), and HOBt (10.2 mmol) in THF (150 ml) is added N-ethyldiiso- propylamine (35 mmol) and the mixture is stirred at room temperature overnight. The mixture is concentrated in vacuo and diluted with ethyl acetate (150 ml). The org. layer is washed with sat. aq. sodium carbonate (3x) and water (2x), dried over sodium sulfate, and evaporated in vacuo. Flash chromatography (silica, petroleum ether/ ethyl acetate 1:1 ⁇ ethyl acetate / MeOH 49:1) afforded the product.
  • step C (5 mmol) in toluene/n-butanol/glacial acetic acid 5:5:1 (200 ml) is heated to reflux for 24 h, concentrated in vacuo, and diluted with ethyl acetate (200 ml).
  • the org. layer is washed with sat. aq. sodium carbonate (2x) and water (1x), dried over sodium sulfate, and evaporated in vacuo. Flash chromatography (silica, petroleum ether/ethyl acetate 3:1 - 1 :3) afforded the product.
  • step D (20 mmol) in dichloromethane (180 ml) is added dropwise trifluoroacetic acid (180 mmol) and the mixture is stirred overnight.
  • the yellow solution is added dropwise to sat. aq. sodium carbonate (190 mmol) and the mixture is stirred for another 30 min.
  • the org. layer is separated, dried over sodium sulfate, and concentrated in vacuo. Flash chromatography (silica, dichloromethane / MeOH 20:1 ) gave final products of formula (la), see table I (examples 1 to 8).
  • step C (3.08 mmol) in THF (50 ml) is added N-ethyldiisopropylamine (6 mmol) followed by Boc anhydride (3.5 mmol) and the mixture is stirred at room temperature for 1 h.
  • the org. layer is diluted with ethyl acetate (50 ml) and extracted with water (2x40 ml). The org. layer is separated and dried over sodium sulfate. Flash chromatography (silica, ethyl acetate/petroleum ether 3:1 ⁇ ethyl acetate) afforded the Boc-protected intermediate.
  • N-Boc-Deprotection is achieved according to procedure E, step E to give the final products of formula (lb), see table III, examples 9 to 10.
  • step D (20 mmol) in MeOH (150 ml) is hydrogenated (50 psi) in the presence of Pd/C (10%) at 50°C for 90 min.
  • the catalyst is removed by filtration and the filtrate is concentrated in vacuo.
  • Trituration (dichloro- methane/ether/petroleum ether) and drying under high vacuum yields the final products of general formula (Id), see table VI, examples 21 to 25.
  • step A (2 mmol) and general procedure G, step A (4 mmol) in THF (60 ml) is added N-ethyldiisopropylamine (4.8 mmol) and the mixture is heated to reflux for 5 h and then stirred at room temperature overnight. The mixture is concentrated in vacuo, diluted with ethyl acetate (100 ml). The org. layer is washed with sat. aq. sodium bicarbonate, dried over sodium sulfate, and evaporated in vacuo. Flash chromatography (silica, ethyl acetate/petroleum ether 3:1 -» 2:1) afforded the product.
  • step B (2 mmol) in dichloromethane (50 ml) is added TFA (4.5 ml) and the mixture is stirred at room temperature for 3 h. The mixture is neutralized with sat. aq. sodium bicarbonate (250 ml) and the aq. layer is extracted with dichloromethane (4x150 ml). The combined org. layers are dried over sodium sulfate and evaporated in vacuo to give the final products of formula (lc), see table IV, examples 11 to 20.
  • step A (4.5 mmol) and N-ethyldiisopropylamine (9 mmol) in dichloromethane (90 ml) is added at 0°C the product of general procedure G, step D (6.75 mmol) and the mixture is stirred at 0°C for 30 min., at room temperature for 2 h, and heated to refluxovemight.
  • the mixture is diluted with dichloromethane (100 ml), the org. layer is washed with sat aq. sodium bicarbonate, and dried over sodium sulfate. Flash chromatography (silica, ethyl acetate / petroleum ether 1:2) afforded the product.
  • step E-G (3 mmol) and aldehyde (12 mmol) in THF (120 ml) is added p-toluenesulfonic acid hydrate (3.6 mmol) and sodium triacetoxyborohydride (12.5 mmol) and the mixture is stirred at room temperature for 48 h. Sat. aq. sodium bicarbonate (100 ml) is added, the mixture is stirred for another 30 min., and then extracted with ether (3x100 ml). The combined org. layers are dried over sodium sulfate and concentrated in vacuo. Flash chromatography (silica, ethyl acetate) and trituration (ether / petroleum ether)afforded the product.
  • step E-G (4 mmol) and aldehyde (4 mmol) in THF (100 ml) is added p-toluenesulfonic acid hydrate (4 mmol) and sodium triacetoxyborohydride (8.3 mmol) and the mixture is stirred at room temperature for 2 h. Sat. aq. sodium bicarbonate (100 ml) is added, the mixture is stirred for another 30 min., and then extracted with ether (4x100 ml). The combined org. layers are dried over sodium sulfate and concentrated in vacuo. Flash chromatography (silica, dichloromethane/MeOH 20:1) afforded the product
  • Step E Acylation using free carboxylic acids
  • step E to G (0.6 mmol), the corresponding carboxylic acid (0.6 mmol), TBTU (0.615 mmol), and HOBt (0.615 mmol) in THF (15 ml) is added at room temperature N-ethyldiisopropylamine (2.1 mmol) and the mixture is stirred overnight. The mixture is diluted with ethyl acetate (100 ml), extracted with sat. aq. sodium bicarbonate (100 ml), and dried over sodium sulfate. Flash chromatography (silica, dichloromethane / MeOH 49:1 ⁇ 19:1) gave the product.
  • step C (0.7 mmol) and the corresponding acid chloride (0.77 mmol) in dichloromethane (20 ml) is added at room temperature N-ethyldiisopropylamine (2.1 mmol) and the mixture is stirred overnight The mixture is diluted with dichloromethane (100 ml), extracted with sat. aq. sodium bicarbonate (100 ml), and dried over sodium sulfate. Flash chromatography (silica, dichloromethane / MeOH 49:1 ⁇ 19:1) gave the product.
  • step C (3 mmol) in MeOH (150 ml) is hydrogenated (50 psi) in the presence of Pd/C (10%) at 50°C for 90 min.
  • the catalyst is removed by filtration and the filtrate is concentrated in vacuo.
  • step D to F (3 mmol) in MeOH (150 ml) is hydrogenated (50 psi) in the presence of Pd/C (10%) at 50°C for 90 min.
  • the catalyst is removed by filtration and the filtrate is concentrated in vacuo. Trituration (dichloromethane / ether / petroleum ether) and drying under high vacuum yielded the product.
  • step C (2 mmol) in dichloromethane (18 ml) is added dropwise trifluoroacetic acid (18 mmol) and the mixture is stirred overnight.
  • the yellow solution is added dropwise to sat. aq. sodium carbonate (19 mmol) and the mixture is stirred for another 30 min.
  • the org. layer is separated, dried over sodium sulfate, and concentrated in vacuo Purification by HPLC (ZorbaxSB-C18 (5 ⁇ m) column, gradient of water / MeCN + 0.1% formic acid, detection at 254 nm and 230 nm) and lyophilization afforded the product.
  • step D to F (2 mmol) in di- chloromethane (18 ml) is added dropwise trifluoroacetic acid (18 mmol) and the mixture is stirred overnight.
  • the yellow solution is added dropwise to sat. aq. sodium carbonate (19 mmol) and the mixture is stirred for another 30 min.
  • the org. layer is separated, dried over sodium sulfate, and concentrated in vacuo. Purification by HPLC (ZorbaxSB-C18 (5 ⁇ m) column, gradient of water/MeCN + 0.1% formic acid, detection at 254 nm and 230 nm) and lyophilization afforded the product.
  • Examples 26 and 27 Compounds of general formula (le) is synthesised on an ACT 440XT MOS robot according to general procedure A using as first building block (step A) Fmoc-D-Lys(Boc)-OH, Fmoc-D-Arg(Pbf)-OH, Fmoc-L-Lys(Boc)-OH or Fmoc L-Arg(Pbf)-OH.
  • first building block step A
  • Fmoc-D-Lys(Boc)-OH Fmoc-D-Arg(Pbf)-OH
  • Fmoc-L-Lys(Boc)-OH Fmoc L-Arg(Pbf)-OH
  • Benzaldehyde, 2- naphthylaldehyde, biphenyl-4-carbaldehyde or 4-benzyloxy-benzaldehyde is used as second building block (step C).
  • the third building block (step D) is covered by Boc-D-Phe-OH, Boc- tf-(2-naphthyl)-L-Ala-OH, Boc-D-Ser(Bzl)-OH, Boc-#-(2-naphthyl)-D-Ala-OH, Boc-L-Phe-OH, or Boc-L-Ser(Bzl)-OH. 24 random samples are analysed using HPLC-MS method B.
  • Stereo pos 3 and 6 Absolute stereochemistry at the position 3 and 6, respectively, of the diketopiperazin ring system
  • the purified product from step B is dissolved in 50 mi DCM and 50 ml TFA is added.
  • the solvents are removed after 1 h.
  • the residual oil is taken up in 50 mi DCM and 1 ml
  • DIPEA is added. Another 1 ml of DIPEA is added after 1 h and again after an additional 90 min. The solvent is removed in vacuo and the product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril. The product is freeze dried from 0.1 N HCl in water.
  • Step B The intermediate from example 28, Step A is used.
  • the purified product from step B is dissolved in 100 ml DCM and 100 ml TFA is added. The solvents are removed in vacuo after 30 min. The residual oil is taken up in 100 ml DCM and
  • 2-terf-Butoxycarbonylamino-3-(2-naphtyl)propionic acid (5.00 g, 15.85 mmol) is dissolved in 100 ml of tetrahydrofuran in a 500 ml flask equipped with a magnetic stirrer.
  • reaction is added to 200 ml of ethyl acetate and washed with a mixture of 25 ml of water and 25 ml of aqueous sodium hydrogen carbonate (saturated).
  • aqueous phase is extracted with 100 ml of ethyl acetate.
  • the combined organic phases are then washed with 50 ml of aqueous sodium hydrogen sulfate (10%), 50 ml of brine, dried over magnesium sulfate and filtered.
  • the reaction is added to 100 ml of dichloromethane and washed with 30 ml of brine, 3x50 ml of aqueous phosphate buffer (pH 6.6), 50 ml of brine, dried over magnesium sulfate, filtered and concentrated in vacuo to afford a crude oil which is purified by preparative HPLC (20-40% CH 3 CN in water/0.1 % trifluoroacetic acid, 40 min). The obtained pure fractions are combined and 1 ml of 1N aqueous hydrogen chloride is added. The compound is lyophilized to give 60.1 mg (14%) of the title compound as a hydrochloride-salt.
  • Step A The intermediate from example 28, Step A is used.
  • Example 34 The purified product from step B is dissolved in 50 ml DCM and 50 ml TFA is added. The solvents are removed in vacuo after 45 min. The residual oil is taken up in 50 ml DCM and 3.0 ml DIPEA is added. The solvent is removed in vacuo after 2.3 h and the product is purified on a C18 reverse phase column (
  • Step A The intermediate from example 39, Step A is used.
  • Step B The intermediate from example 39, Step A is used.
  • Step A The intermediate from example 39, Step A is used.
  • Step B The intermediate from example 39, Step A is used.
  • Step B The intermediate from example 39, Step A is used.
  • the purified product from step B is dissolved in 25 ml DCM and 25 ml TFA is added. The solvents are removed in vacuo after 30 min. The residual oil is taken up in 25 ml DCM and 2.0 ml DIPEA is added. The solvent is removed in vacuo after 1 h and the product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • Triphenylphosphine (356 mg, 1.4 mmol) and cyclohexanol (136 mg, 1.4 mmol) is added to a solution of the product from step B (300 mg, 0.45 mmol) in THF (20 ml) with stirring at room temperature under nitrogen.
  • a solution of diethyl azodicarboxylate (214 ml, 1.4 mmol) in THF (5 ml) is added dropwise during 30 min while the temperature is kept below 30 °C with cooling on an ice-bath. After stirring at room temperature for about 3 days the mixture is evaporated to dryness and purified on silica with ethyl acetate/heptane (1 :3) affording a crude product, which is used in the next step without further purification.
  • step C The product from step C (50 mg, 0.067 mmol) is dissolved in DCM (10 ml) and TFA (5 ml) is added. The solution is stirred for 2 h at room temperature. After evaporation in vacuo the residue is taken up in toluene (10 ml) and the solvent is again removed in vacuo. The residue is now dissolved in DCM (10 ml) and ⁇ /, ⁇ /-diisopropylethylamine (100 ⁇ l, 0.57 mmol) is added.
  • Triphenylphosphine (356 mg, 1.4 mmol) and 3-trifluoromethylcyclohexanol (235 mg, 1.4 mmol) is added to a solution of the product from step B in example 44 (312 mg, 0.456 mmol) in THF (20 ml) with stirring at room temperature under nitrogen.
  • a solution of diethyl azodicarboxylate (214 ml, 1.4 mmol) in THF (5 ml) is added dropwise during 30 min while the temperature is kept below 30 °C with cooling on an ice-bath.
  • step A The product from step A (202 mg, 0.24 mmol) is dissolved in DCM (15 ml) and TFA (15 ml) is added. The solution is stirred for 6 h at room temperature. After evaporation in vacuo the residue is taken up in toluene (10 ml) and the solvent is again removed in vacuo. The residue is now dissolved in DCM (20 ml) and ⁇ /, ⁇ /-diisopropylethylamine (83 ⁇ l, 0.48 mmol) is added. After stirring overnight, the mixture is evaporated in vacuo and the residue is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1 %TFA in water and.
  • step B The product from step B is dissolved in DCM (30 ml) followed by the addition of TFA (10 ml). The solution is stirred for 2 h at room temperature. After evaporation in vacuo the residue is taken up in toluene (30 ml) and the solvent is again removed in vacuo. The residual oil is now dissolved in DCM (20 ml) and ⁇ /,/V-diisopropylethylamine (0.98 ml, 5.6 mmol) is added.
  • Step A 0.123 g (0.25 mmol) of (S,S)-6-(4-amino-butyl)-1-biphenyl-4-ylmethyl-3-naphthalen-2- ylmethyl-piperazine-2,5-dione (example 11) is mixed with 1 ml of tetrahydrofuran, 0.288 ml (3.8 mmol) of 37% formalin solution, and 0.045 ml of acetic acid. The mixture is stirred for 30 minutes. 0.027 g (0.425 mmol) of sodium cyanoborohydride is added, followed by 1 ml of tetrahydrofuran and 1 ml of methanol.
  • 0.169 g (0.250 mmol) of the sulfonamide obtained by step A is mixed with 0.021 g (0.150 mmol) of potassium carbonate, 0.6 ml of dimethylformamide, and 0.036 ml (0.575 mmol) of methyl iodide. The mixture is stirred for 22 hours. The methyl iodide is evaporated off.
  • step B The suspension obtained by step B is treated with 0.069 g (0.50 mmol) of potassium carbonate, 0.30 ml of dimethylformamide, and 0.070 ml (1.0 mmol) of 2-mercaptoethanol and stirred for four hours.
  • the mixture is partitioned between 40 ml of ethyl acetate and 20 ml of 0.2 M aqueous sodium hydroxide.
  • the organic phase is washed with 0.2 M aqueous sodium hydroxide (2x20 ml) and water (30 ml). Drying over sodium sulfate, filtration and evaporation afforded 0.141 g of a tough yellow residue.
  • Step C 5.0 mmol, 1.6 g Boc-Tyr(Et)-OH is dissolved in 15 ml THF, 0.5 equi., 390 ⁇ l DIC is added and the resulting mixture is stirred for 35 min. Then 2.5 mmol of the crude product of step A is added in 15 ml THF. After 4 h 430 ⁇ l DIPEA is added and the mixture is stirred overnight. The solvent is removed in vacuo and the residue is taken up in 60 ml ethyl acetate. The org. phase is washed twice with 30 ml 1 M HCl and twice with 30 ml sat. NaHCO 3 and dried over sodium sulfate. The solvent is removed in vacuo and the residual oil is purified on silica with ethyl acetate/heptane (2:3). Step C:
  • the purified product from step B is dissolved in 30 ml DCM and 30 ml TFA is added. The solvents are removed in vacuo after 30 min. The residual oil is taken up in 30 ml DCM and
  • the residual oil is purified on silica with ethyl acetate:heptane 2:3.
  • the pure product is dissolved in 100 ml DCM and 100 ml TFA.
  • the solvent is removed after 15 min and the oil taken up in 150 ml DCM and 5 ml DIPEA is added and the mixture stirred at room temperature. After 20 min another 5 ml DIPEA are added and again after 3 h and 5 h.
  • the solvent is removed in vacuo after 6 h and used for unpurified for the next step.
  • Step B The product of step A (14 mmol) is dissolved in 100 ml DCM and 2 equi, 6.1 ml Boc- anhydrid and 1 equi., 2.45 ml DIPEA are added. The solvent is removed in vacuo and the product is purified on silica using ethyl acetate.
  • Step C The product of step A (14 mmol) is dissolved in 100 ml DCM and 2 equi, 6.1 ml Boc- anhydrid and 1 equi., 2.45 ml DIPEA are added. The solvent is removed in vacuo and the product is purified on silica using ethyl acetate.
  • Step C The product of step A (14 mmol) is dissolved in 100 ml DCM and 2 equi, 6.1 ml Boc- anhydrid and 1 equi., 2.45 ml DIPEA are added. The solvent is removed in vacuo and the product is purified on silica using
  • step C 0.5 mmol, 0.3 g of the product of step C is dissolved in 25 ml DCM and 25 ml TFA. The solvent is removed in vacuo after 20 min and the product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • step B 0.5 mmol, 0.3 g of the product of step B is dissolved in 5 ml THF. 1.5 equi., 0.2 g triphenylphosphine and 1.5 equi., 58 ⁇ l 2-propanol are added. The reaction is started by adding 1.5 equi., 120 ⁇ l diethyl azadicarboxylate. The mixture is stirred over night at room temperature. The product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1%) TFA in water and acetonitril.
  • Example 53 General procedure (D))
  • step B 0.5 mmol, 0.3 g of the product of step B is dissolved in 4 ml THF. 1.5 equi., 0.2 g triphenylphosphine in 1 ml THF and 1.5 equi., 61 ⁇ l cyclopropyl methanol are added. The reaction is started by adding 1.5 equi., 120 ⁇ l diethyl azadicarboxylate. The mixture is stirred over night at room temperature. The product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • 0.5 mmol, 0.3 g of the product of step B is dissolved in 5 ml THF.
  • 1.5 equi., 0.2 g triphenylphosphine in 1 ml THF and 1.5 equi., 85 mg cyclohexanol in 1 ml THF are added.
  • the reaction is started by adding 1.5 equi., 120 ⁇ l diethyl azadicarboxylate. The mixture is stirred over night at room temperature.
  • the product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • Step A The intermediate of example 50, step B is used.
  • Step B The intermediate from example 56, Step A, is used Step B:
  • step B 0.5 mmol, 0.3 g of the product of step B is dissolved in 5 ml THF. 1.5 equi., 0.2 g triphenylphosphine and 1.5 equi., 31 ⁇ l methanol are added. The reaction is started by adding 1.5 equi., 120 ⁇ l diethyl azadicarboxylate. The mixture is stirred over night at room temperature. The product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • step C 0.4 mmol, 0.2 g of the product of step C is dissolved in 10 ml DCM and 10 ml TFA. The solvent is removed in vacuo after 15 min and the product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • Step C 0.5 mmol, 0.3 g of the product of step B is dissolved in 5 ml THF. 1.5 equi., 0.2 g triphenylphosphine in 1 ml THF and 1.5 equi., 44 ⁇ l ethanol are added. The reaction is started by adding 1.5 equi., 120 ⁇ l diethyl azadicarboxylate. The mixture is stirred over night at room temperature. The product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1 % TFA in water and acetonitril. Step D:
  • the residual oil is purified on silica with ethyl acetate:heptane 2:3.
  • the pure product is dissolved in 100 ml DCM and 100 ml TFA.
  • the solvent is removed after 20 min and the oil taken up in 100 ml DCM and 5 ml DIPEA is added and the mixture stirred at room temperature. After 45 min another 5 ml DIPEA are added and again after 2 h.
  • the solvent is removed in vacuo after 3 h and the crude product used in the next step.
  • step A The product of step A (13 mmol) is dissolved in 100 ml DCM and 2 equi, 5.5 ml Boc- anhydrid and 1 equi., 2.2 ml DIPEA are added. The solvent is removed in vacuo after 2 hand the product is purified on silica using ethyl acetate.
  • step C 0.5 mmol, 0.3 g of the product of step C is dissolved in 25 ml DCM and 25 ml TFA. The solvent is removed in vacuo after 20 min and the product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1 % TFA in water and acetonitril.
  • Step B A mixture of the product of step A, Cu(OAc) 2 (1 equi), pyridine-3-boronic acid (2 equi), pyridine (5 equi) and crushed molecular sieves (4 A) in dichloromethane are stirred under an air atmosphere for 72 h, filtered through a plug of silica and purified by flash chromatography (eluant ethyl acetate/heptane). Addition of 20 ml dichloromethane and 3 ml trifluoroacetic acid per 500 mg compound removed the Boc protecting group and after purification by reverse phase HPLC (water, actetonitrile, trifluoroactetic acid eluant) afforded the title compound.
  • Step A To a solution of H-Lys(Boc)-OMe HCl (5.0 g, 16.7 mmol) in THF (150 ml) is added 4- bromobenzaldehyde (3.1 g, 16.7 mmol) and ⁇ /, ⁇ /-diisopropylethylamine (3.0 ml, 16.7 mmol), and the mixture is stirred in the presence of powdered molecular sieves (4 A) for 4 h at room temperature. Then methanol (17 ml), acetic acid (8.0 ml) and sodium cyanoborohydride (3.1 g, 50 mmol) is added and the mixture is stirred for two days at room temperature.
  • step B The intermediate of example 71, step B is used.
  • step B 0.5 mmol, 0.3 g of the product of step B is dissolved in 5 ml THF. 1.5 equi., 0.2 g triphenylphosphine and 1.5 equi., 58 ⁇ l 2-propanol are added. The reaction is started by adding 1.5 equi., 120 ⁇ l diethyl azadicarboxylate. The mixture is stirred for 6 h at room temperature. The product is purified on a C18 reverse phase column (Sep-Pak, Waters, 10 g) with 0.1% TFA in water and acetonitril.
  • Step B (S)-2-terf-Butoxycarbonylamino-3-(9H-fluoren-9-ylmethoxycarbonylamino)propionic acid methyl ester (4.80 g, 10.90 mmol) is dissolved in 20 ml of ethyl acetate in a 250 ml flask equipped with a magnetic stirrer. To the stirred solution is added 80 ml of 2.8 M hydrogen chloride in ethyl acetate and the reaction is stirred for 2 hours under nitrogen. Concentrated in vacuo to give a white solid, which is taken up in ethyl acetate, stirred and filtered.
  • aqueous phase is extracted with 50 ml of ethyl acetate and the combined organic phases are washed with 25 ml of water, 25 ml of brine, dried over magnesium sulfate and filtered. Concentrated in vacuo to give 7.62 g of yellow foam, which is analyzed by LC-MS, indicating only 16 % of (2S)-2-[biphenyl-4-yImethyl-(2S)-(2-fer.-butoxycarbonylamino-3-(2- naphthyl)propionyl)amino]-3-(9H-fluoren-9-ylmethoxycarbonylamino)propionic acid methyl ester.
  • the crude product is dissolved in 50 ml of tetrahydrofuran and 2-fer/ butoxycarbonyl- amino-3-(2-naphtyl)propionic acid (2.32 g, 7.37 mmol), bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (3.44 g, 7.37 mmol) and N-ethyldiisopropylamin (1.26 ml, 7.37 mmol) are added. Stirred overnight and concentrated in vacuo. Taken up in 150 ml of dichloromethane and filtered through Hyflo Super Cel®.
  • the clear filtrate is washed with 50 ml of aqueous sodium hydrogen sulfate (10%), 50 ml of aqueous sodium hydrogen carbonate (saturated), 50 ml of water, and 50 ml of brine, dried over magnesium sulfate and filtered.
  • aqueous phase is extracted 2 times with 20 of dichloromethane, and the combined organic phases are washed with 3 times of 30 ml of aqueous phosphate buffer (pH: 6.6), 20 ml of brine, dried over magnesium sulfate, filtered and concentrated in vacuo to afford 0.50 g (74%) of (3S,6S)-6-Aminomethyl-1-biphenyl-4-ylmethyl-3-(2- naphthyl)methylpiperazine-2,5-dione as yellow foam.
  • Step J To a solution of 4- ⁇ [((2S,5S)-1-biphenyl-4-ylmethyl-5-(2-naphthyl)methyl-3,6-dioxo-piperazin-
  • the compound is lyophilized to give 55 mg (52%) of the title compound as a hydrochloride salt.
  • (2S)-3-terf-butoxycarbonylamino-2-[[(2S)-2-fer.-butoxycarbonylamino-3-(4- ethoxyphenyl)propionyl]-(4-phenoxybenzyl)amino]propionic acid methyl ester (6.08 g, theoretically 7.49 mmol) is dissolved in 100 ml of dichloromethane and 100 ml of 5 trifluoroacetic acid. Stirred for 2 hours, concentrated in vacuo, stripped 2 times from dichloromethane to give a thin orange oil.
  • Step D 5 To a solution of 3S,6S)-(6-aminomethyl-3-(4-ethoxybenzyl)-1 -(4-phenoxybenzyl)piperazine- 2,5-dione (0.24 g, 0.35 mmol) in 10 ml of tetrahydrofuran and 10 ml of methanol is added 4(5)-imidazolecarboxaldehyde (0.10 g, 1.1 mmol), molecular sieves (4A), acetic acid (42 ⁇ l, 0.20 mmol) and sodium cyanoborohydride (1.1 ml, 1.1 mmol). Stirred for 5 days.
  • Step A 288 mg of the boc-protected product of example 75 is dissolved in 10 ml ethanol and
  • the product resin from general procedure C, step A is used. To 0.18 g of this resin are added sequentially a solution of 0.468 mmol Boc-Lys(Fmoc)-OH in 1.6 ml of 1,2- dichloropropane / tetrahydrofuran (1:1), 0.045 ml (0.288 mmol) of diisopropylcarbodiimide, and a solution of 0.036 mmol of 4-dimethylamino pyridine in 0.2 ml of 1 ,2-dichloropropane. The mixture is shaken for 15 hours. The liquids are filtered off and the resin is washed with dimethylformamide (2x2 ml), tetrahydrofuran (2x2 ml), and dichloromethane (2x2 ml).
  • step A The resin obtained by step A is shaken with a mixture of 2.5 ml trifluoroacetic acid/- dichloromethane 1 :1 for one hour. The liquids are filtered off and the resin is washed with tetrahydrofuran (2x2 ml), tetrahydrofuran / ethyldiisopropylamine 3:1 (3x2 ml), methanol (2 ml) and tetrahydrofuran (2 ml).
  • step B To the resin obtained by step B, a solution of 0.36 mmol of 4-phenoxybenzaldehyde in 1.7 ml of 1-methyl-2-pyrrolidone and 0.1 ml of acetic acid are added. The mixture is shaken for three hours. The liquids are filtered off. The resin is shaken with a solution of 0.9 mmol of sodium cyanoborohydride in 1.7 ml of dichloromethane / methanol 1 :1 for one hour. The liquids are filtered off.
  • the resin is washed with methanol (2x2 ml), dichloromethane / methanol 1:1 (2 ml), dichloromethane / ethyldiisopropylamine 19:1 (2x2 ml), and tetrahydrofuran (2x2.5 ml).
  • step C To the resin obtained by step C, a solution of 0.468 mmol of Boc-Tyr(Me)-OH in 1.6 ml of 1 ,2-dichloropropane / tetrahydrofuran 1:1 is added, followed by a solution of 0.288 mmol of diisopropylcarbodiimide in 0.2 ml of 1 ,2-dichloropropane. The mixture is shaken for 30 minutes. 0.043 ml (0.252 mmol) of ethyldiisopropylamine is added, and shaking is continued for 14 hours. The liquids are filtered off and the resin is washed with tetrahydrofuran (2x2.5 ml).
  • step D The resin obtained by step D is shaken with a mixture of 1.5 ml of dimethylformamide and 0.5 ml of piperidine for 30 min. The liquids are filtered off and the resin is washed with dimethylformamide (2x2 ml) and tetrahydrofuran (2x3 ml).
  • step E To the resin obtained by step E, a suspension of 0.36 mmol of imidazole-2- carbaldehyde in 1.8 ml of 1-methyl-2-pyrrolidone / tetrahydrofuran 17:1 is added, followed by 0.1 ml of acetic acid. The mixture is shaken for 2.5 hours. The liquids are filtered off and the resin is washed with dichloromethane (4x2 ml). A solution of 0.90 mmol of sodium cyanoborohydride in 1.7 ml of dichloromethane / methanol 1 :1 and 0.05 ml of acetic acid are added and the mixture is shaken for one hour.
  • step F The resin obtained by step F is shaken with 2.5 ml of dichloromethane / trifluoroacetic acid 1 :1 for 30 minutes. The liquids are filtered off and the resin is washed with dichloromethane (2x2 ml), tetrahydrofuran (2x2.5 ml), and methanol (2x2.5 ml).
  • step G To the resin obtained by step G, 2.0 ml of dichloromethane and 1.0 ml of 40% methylamine in methanol are added. The mixture is shaken for 3.5 hours. The mixture is filtered and the filtrate is collected. The resin is washed with 3.5 ml of dichloromethane / methanol 6:1 and the washing filtrate is collected. Both filtrates are mixed and evaporated to give a residue.
  • step H The residue obtained by step H is dissolved in a mixture of 4.8 ml of water, 3.2 ml of acetonitrile and 0.8 ml of 1M aqueous hydrochloric acid and purified by HPLC. Addition of dilute aqueous hydrochloric acid and freeze-drying afforded 12.2 mg of the product.
  • step F a solution of pyridine-2-carbaldehyde is used instead of the imidazole-2-carbaldehyde suspension.
  • step H The residue obtained by step H is dissolved in a mixture of 4.8 ml water, 3.2 ml of acetonitrile and 0.8 ml of 1M aqueous hydrochloric acid and purified by HPLC. Addition of dilute aqueous hydrochloric acid and freeze-drying afforded 20.6 mg of the product.
  • Step B To a solution of -(1 R)- ⁇ [(2S,5S)-5-(4-ethoxybenzyl)-3,6-dioxo-1 -(4-phenoxybenzyl)piperazin- 2-ylmethyl]carbamoyl ⁇ ethyl)imidazole-1 -carboxylic acid tert-butyl ester (theoretically 0.35 mmol) in 5 ml of dichloromethane is added 5 ml of trifluoroacetic acid. Stirred for 2 hours, concentrated in vacuo and purified by preparative HPLC (23-43% acetonitrile in water /0.1% trifluoroacetic acid, 40 min). To the combined pure fractions are added 2 ml of 1 M aqueous hydrogen chloride and the mobile phase is removed by lyophilisation to afford 88.1 mg of the title compound.
  • Step B 1.4 g (3.9 mmol) Boc-Tyr(tBu)-OH are dissolved in 20 ml THF. 300 ⁇ l diisopropylcarbodiimide are added and the the mixture is stirred for 1 h.
  • the crude product from step A is added in 10 ml THF. After 2.5 h 320 ⁇ l DIPEA is added and the reaction is stirred over night. Another 320 ⁇ l DIPEA are added and after 1 h the solvent is removed in vacuo. The residual oil is taken up in 50 ml ethyl acetate.
  • the org. phase is washed twice with 50 ml 1 N HCl, twice with 50 ml sat. sodium hydrogen carbonate and dried over sodium sulfate. The solvent is removed in vacuo and the residual oil is purified on silica using ethyl acetate/heptane 2:3.
  • Step D 0.3 g (0.7 mmol) of the product from step C is dissolved in 15 ml dichlormethane.
  • step B Fmoc-L-Lys(Boc)-OH.
  • step D 2-Phenoxy- benzaldehyde, biphenyl-4-carbaldehyde, benzaldehyde or 4-benzyloxy-benzaldehyde is used as second building block (step D).
  • step E The third building block (step E) is covered by Boc- ? ⁇ (2-naphthyl)-L-Ala-OH, Boc-L-Tyr(bz)-OH, Boc-L-Trp(Boc)-OH, Boc-£-(1-naphthyl)-L-Ala-OH, Boc-L-Bip-OH or Boc-L-Phe-OH, samples are analysed using HPLC-MS method D.
  • Stereo pos 3 and 6 Absolute stereochemistry at the position 3 and 6, respectively, of the diketopiperazin ring system
  • step G (196 mg, 0.4 mmol) in DMF (5 ml) is added pyrazole-1-carboxamidine hydrochloride (60 mg, 0.41 mmol) and the mixture is stirred at room temperature overnight. Ether is added and the white precipitate collected by filtration. The precipitate is washed repeatedly with ether and dried under high vacuum to give the product (186 mg, 82%).
  • ESl-MS: (M+CI) " 570.
  • step G (100 mg, 0.2 mmol) and 2-chloro-3-nitro-pyridine (40 mg, 0.25 mmol) in DMF (1 ml) is added N-ethyldiisopropylamine (0.07 ml, 0.4 mmol) and the mixture is stirred at room temperature for 72 h. The mixture is diluted with ice water (50 ml) and the precipitate is collected by filtration. Flash chromatography (silica, dichloromethane / MeOH 30:1) gave the corresponding 3-nitropyridyl intermediate (90 mg, 73%).
  • ESl-MS: (M+Hf 630
  • step G (150 mg, 0.295 mmol) and chloroacetonitrile (0.02 ml, 0.313 mmol) in EtOH (1.5 ml) is heated to reflux for 3 h. Chloroacetonitril (0.01 ml) is added and the mixture is heated for another 2 h. The mixture is concentrated in vacuo and the residue purified by flash chromatography (silica, dichloromethane / MeOH 20:1) to give the product (80 mg, 50%).
  • ESl-MS: (M+Hf 547
  • step D 300 mg, 0.44 mmol
  • acetic anhydride 0.085 ml, 0.90 mmol
  • step D (300 mg, 0.44 mmol) and cyclohexanecarboxaldehyde (0.12 ml, 0.99 mmol) in THF (20 ml) is added glacial acetic acid (0.06 ml) and the mixture is stirred for 1 h.
  • Sodium triacetoxyborohydride (240 mg, 1.076 mmol) is added and the mixture is stirred for 3 days. Sat. aq. sodium bicarbonate is added, the mixture stirred for 30 min., and then extracted with ether (3x70 ml). The combined org.
  • Step 2 The Cbz-protected intermediate (250 mg, 0.322 mmol) in MeOH (30 ml) is hydrogenated (50 psi) in the presence of Pd/C (10%) at 50°C for 1 h. The catalyst is removed by filtration and the filtrate is concentrated in vacuo. The residue is triturated (di- chloromethane/ether) to give the product (125 mg, 60%).
  • ESl-MS: (M+Hf 643.
  • Step l
  • step D To the corresponding Cbz-protected product from general procedure G, step D (300 mg, 0.44 mmol) and acetaldehyde (100 mg, 2.27 mmol) in THF (20 ml) is added glacial acetic acid (0.06 ml) and the mixture is stirred for 1 h. Sodium triacetoxyborohydride (240 mg, 1.076 mmol) is added and the mixture is stirred for 3 days. Sat. aq. sodium bicarbonate is added, the mixture stirred for 30 min., and then extracted with ether (3x70 ml). The combined org.
  • Step 2 The Cbz-protected intermediate (250 mg, 0.322 mmol) in MeOH (30 ml) is hydrogenated (50 psi) in the presence of Pd/C (10%) at 50°C for 1 h. The catalyst is removed by filtration and the filtrate is concentrated in vacuo. The residue is triturated (dichloromethane / ether) to give the product (56 mg, 41%).
  • ESl-MS: (M+Hf 575.
  • Step l
  • step D 300 mg, 0.44 mmol and 4-pyridylcarbaldehyde (100 mg, 0.934 mmol) in THF (20 ml) is added glacial acetic acid (0.06 ml) and the mixture is stirred for 1 h.
  • Sodium triacetoxyborohydride 240 mg, 1.076 mmol is added and the mixture is stirred for 3 days.
  • Another portion of 4- pyridinecarboxaldehyde (100 mg, 0.934 mmol), glacial acetic acid (0.06 ml), and sodium triacetoxyborohydride (240 mg, 1.076 mmol) is added and the mixture is stirred for another 2 days. Sat.
  • step D (240 mg, 0.353 mmol), 3-N-Cbz-aminopropionic acid (240 mg, 1.075 mmol), HOBt (140 mg, 1.034 mmol), and TBTU (340 mg, 1.06 mmol) in THF (15 ml) is added at room temperature N-ethyldiisopropylamine (0.2 ml, 1.148 mmol) and the mixture is stirred overnight. Sat. aq. sodium bicarbonate (40 ml) is added, the mixture stirred for 30 min., and then extracted with dichloromethane (3x70 ml). The combined org.
  • step D 300 mg, 0.441 mmol
  • N-Boc-piperidin-4-yl carboxylic acid 125 mg, 0.545 mmol
  • HOBT 70 mg, 0.517 mmol
  • TBTU TBTU
  • step D is added at room temperature N-ethyldiisopropylamine (0.1 ml, 0.57 mmol) and the mixture is stirred overnight. Sat. aq. sodium bicarbonate (40 ml) is added, the mixture stirred for 15 min., and then extracted with dichloromethane (3x70 ml). The combined org.

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Abstract

La présente invention concerne de nouveaux composés de la formule générale (I) ainsi que tout isomère optique ou géométrique ou toute forme tautomère de ce dernier, ou leur sel pharmaceutiquement acceptable. L'invention concerne également leur utilisation comme agonistes des récepteurs mélanocortine, notamment comme agonistes du récepteur MC4. On peut utiliser ces composés, par exemple, dans le traitement de l'obésité.
PCT/DK2003/000797 2002-11-22 2003-11-20 Composes destines au traitement de l'obesite WO2004048345A2 (fr)

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CA002506843A CA2506843A1 (fr) 2002-11-22 2003-11-20 Composes destines au traitement de l'obesite
AU2003281978A AU2003281978A1 (en) 2002-11-22 2003-11-20 2,5-diketopiperazines for the treatment of obesity
JP2004554239A JP2006515574A (ja) 2002-11-22 2003-11-20 肥満症の治療に使用される化合物
EP03773584A EP1572669A2 (fr) 2002-11-22 2003-11-20 2,5-dikétopiperazines pour le traitement de l'obesite

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